Teams at ICON plc

Support clinical study operations including eTMF and CTMS setup and maintenance, document control, trial registrations, meeting coordination, finance and vendor tracking, monitoring oversight, clinical supplies coordination, QC of TMF, and support during audits and inspections per ICH/GCP and sponsor SOPs.

Support clinical study operations including eTMF and CTMS setup and maintenance, document control, sponsor and regulatory compliance (ICH/GCP), trial registration, finance tracking, monitoring visit oversight, supplies coordination, meeting coordination and minute-taking, logs and trackers maintenance, and audit/inspection support.

The Senior Clinical Research Associate will manage site activities and ensure compliance during Oncology clinical trials, focusing on data integrity and subject safety.